Spinous Process Spacer

ABSTRACT

Interspinous process implants are disclosed. Also disclosed are systems and kits including such implants, methods of inserting such implants, and methods of alleviating pain or discomfort associated with the spinal column.

CROSS REFERENCE TO RELATED APPLICATIONS

The present application is a continuation application claiming priorityto U.S. patent application Ser. No. 11/366,388 filed on Mar. 3, 2006,which claims priority to U.S. Provisional Patent Application Ser. No.60/689,532 filed on Jun. 13, 2005, the entire contents of which areincorporated herein by reference.

FIELD OF THE INVENTION

The present invention is generally directed to interspinous processimplants, systems and kits including such implants, methods of insertingsuch implants, and methods of treating spinal stenosis or foralleviating pain or discomfort associated with the spinal column.

BACKGROUND OF THE INVENTION

Occurrences of spinal stenosis are increasing as society ages. Spinalstenosis is the narrowing of the spinal canal, lateral recess or neuralforamen, characterized by a reduction in the available space for thepassage of blood vessels and nerves. Clinical symptoms of spinalstenosis include extremity pain, radiculopathy, sensory or motordeficit, bladder or bowel dysfunction, and neurogenic claudication. Painassociated with such stenosis can be relieved by surgical ornon-surgical treatments, such as medication, physical therapy, backbraces and the like.

There is a need for implants that may be placed between spinal processesfor minimally invasive surgical treatment of spinal stenosis.

SUMMARY OF THE INVENTION

The present invention is directed to minimally invasive implants, inparticular, interspinous process implants or spacers. The invention isfurther directed to systems and kits including such implants, methods ofinserting such implants, and methods of alleviating pain or discomfortassociated with the spinal column.

The present invention provides spacers or implants and methods forrelieving pain and other symptoms associated with spinal stenosis, byrelieving pressure and restrictions on the blood vessels and nerves.Such alleviation of pressure may be accomplished in the presentinvention through the use of an implant placed between the spinousprocess of adjacent vertebra. While the implants and methods of theinvention particularly address the needs of the elderly, the inventioncan be used with individuals of all ages and sizes where a spacerbetween spinous processes would be beneficial.

In certain aspects of the invention, various implants are provided forcreating, increasing, or substantially maintaining a desired distractionor spacing between a first spinous process and a second spinous process(adjacent spinous processes). In another aspect of the invention,implants may be extended to create, increase or substantially maintain adesired distraction or spacing of more than two adjacent spinousprocesses.

In another aspect of the invention, implants in accordance with thepresent invention may be attached to one or more spinous processes orother portion of the spine, or may attach to itself in such a manner asto secure the implant between two adjacent spinous processes. In yetother aspects of the invention, implants in accordance with the presentinvention may be secured in place with respect to spinous processes bymechanical forces resulting from the design of the implant orattachments to the implant, and/or surface modifications thereto.

In another aspect of the present invention, methods are provided fortreating spinal stenosis. In yet further aspects of the invention,methods are provided for inserting implants. These methods may includeimplanting a device to create, increase, or maintain a desired amount ofdistraction between adjacent first and second spinous processes. Methodsmay include creating an incision in a patient, removing any interspinousligaments in a position in which the implant is to be placed in thepatient, sizing the space between adjacent spinous processes, andinserting an implant of the appropriate size between the spinousprocesses. In another aspect of the invention, methods may furtherinclude securing the implant. In another aspect of the invention,methods of the present invention may include distracting the spinousprocesses apart from one another before sizing and/or before insertingthe implant.

In a further aspect of the invention kits are provided that include oneor more implants, and optionally any tools or devices that may berequired or useful in inserting the implant into a patient, such astools or devices that may be useful in distracting spinous processes,and/or selecting, inserting, positioning, and/or securing one or moreimplants.

In a further aspect of the invention systems are provided that includeat least one implant and at least one fastening device. Systems inaccordance with the present invention may further include one or more ofthe following: a tool or device for removing any interspinous ligamentsin the way of inserting the implant; a tool or device for sizing thespace between adjacent spinous processes; and a tool or device fordistracting spinous processes, and/or selecting, inserting, positioning,and/or securing one or more implants.

BRIEF DESCRIPTION OF THE DRAWINGS

The invention will be more readily understood with reference to theembodiments thereof illustrated in the attached figures, in which:

FIGS. 1 a-1 b depict one embodiment of an implant according to thepresent invention for creating, increasing, or maintaining distractionbetween adjacent spinous processes;

FIG. 1 c is a perspective view of the implant of FIGS. 1 a and 1 b;

FIG. 1 d is a side view of the implant of FIGS. 1 a-1 c shown in a firstimplantation position in relation to the spinous processes between whichthe implant is implanted;

FIG. 1 e is a side view of the implant of FIGS. 1 a-1 c shown in asecond implantation position in relation to the spinous processesbetween which the implant is implanted;

FIG. 1 f depicts a stapler that may be used to secure an implant to oneor more spinous processes;

FIG. 1 g depicts a device that may be used to determine a space betweenspinous processes and/or a desired size or shape of implant to be used;

FIGS. 2 and 3 a-3 c depict implants according to other embodiments ofthe present invention;

FIGS. 4 a-4 b depict a perspective and side view of implants accordingother embodiments of the present invention;

FIGS. 5, 6 a, and 7 depict a side view of implants according to otherembodiments of the present invention in relation to the spinal processesbetween which the implants are implanted, where the implants are securedto the spinous processes by a fastening device;

FIG. 6 b depicts a front view of the implant according to FIG. 6 a;

FIG. 8 depicts a side view of the implant of FIG. 7, before beingimplanted between spinous processes;

FIG. 9 depicts other embodiments of implants of the invention;

FIG. 10 depicts other embodiments of implants of the invention;

FIG. 11 depicts other embodiments of implants of the invention inrelation to the spinal processes between which the implants areimplanted;

FIG. 12 depicts other embodiments of implants of the invention inrelation to the spinal processes between which the implants areimplanted;

FIGS. 13 a-13 b depict a side and front view of other embodiments ofimplants of the invention, where the side view is depicted in relationto the spinous processes between which the implants are implanted;

FIGS. 14 a-14 b depict a side and front view of other embodiments ofimplants of the invention, where the side view is depicted in relationto the spinal processes between which the implants are implanted;

FIGS. 15 a-15 b depict a side and front view of other embodiments of theinvention, where the side view is depicted in relation to the spinalprocesses between which the implants are implanted;

FIGS. 16-18 depict other embodiments of implants of the invention;

FIGS. 19-21 depict other embodiments of implants of the invention;

FIGS. 22-24 depict embodiments of the present invention in which theimplants are attached to portions of the spine other than a spinousprocess;

FIGS. 25-26 depict other embodiments of implants of the invention;

FIG. 27 a depicts other embodiments of implants of the invention;

FIG. 27 b depicts a side view of the center portion of FIG. 27 a;

FIG. 28 is a perspective view of another embodiment of an implantaccording to the present invention for creating, increasing, ormaintaining distraction between adjacent spinous processes;

FIG. 29 is a front view of the implant of FIG. 28;

FIG. 30 is a cross-sectional view of the implant of FIG. 29 taken alongline 30-30;

FIG. 31 is a bottom view of the implant of FIGS. 28-30;

FIG. 32 is an end view of the implant of FIGS. 28-31;

FIG. 33 is another end view of the implant of FIGS. 28-32;

FIG. 34 is a perspective view of another embodiment of an implantaccording to the present invention;

FIG. 35 is a front view of the implant of FIG. 34;

FIG. 36 is a perspective view of another embodiment of an implantaccording to the present invention;

FIG. 37 is a perspective view of another embodiment of an implantaccording to the present invention;

FIG. 38 is an end view of the implant of FIG. 37;

FIGS. 39-42 are perspective views demonstrating steps according to oneembodiment of a method of installation of the implant of FIGS. 28-32;

FIGS. 43-44 depict one embodiment of a muscle distraction toolconstructed in accordance with the present invention;

FIGS. 45-46 depict one embodiment of a dilation tool constructed inaccordance with the present invention;

FIGS. 47-48 depict one embodiment of a facet reamer tool constructed inaccordance with the present invention;

FIG. 49 is a perspective view of one embodiment of a facet reamer sleevefor use with the reamer tool of FIGS. 47-48; and

FIGS. 50-52 depict one embodiment of a trial assembly constructed inaccordance with the present invention.

DETAILED DESCRIPTION OF THE INVENTION

Embodiments of the invention will now be described. The followingdetailed description of the invention is not intended to be illustrativeof all embodiments. In describing embodiments of the present invention,specific terminology is employed for the sake of clarity. However, theinvention is not intended to be limited to the specific terminology soselected. It is to be understood that each specific element includes alltechnical equivalents that operate in a similar manner to accomplish asimilar purpose.

Implants

The present invention is directed to minimally invasive implants, inparticular, interspinous process spacers. Implants in accordance withthe present invention may come in many shapes and sizes. Theillustrative embodiments provided herein-below provide guidance as tothe many types of implants that may be advantageously used in accordancewith the present invention. In particular, the implants of the presentinvention are adapted such that their insertion technique (includingmethods of the present invention) is minimally invasive, simpler, and/orsafer than previously discussed techniques. Implants according to thepresent invention may be advantageously inserted into a patient as anout-patient procedure.

Embodiments of the present invention include implants adapted to beplaced between first and second adjacent spinous processes. The implantsmay be adapted such that after insertion of an implant into a patient, aportion of the implant maintains a desired amount of distraction orspacing between two adjacent spinous processes. The implants or portionsthereof that substantially maintain a desired spacing between spinousprocesses are also referred to herein as “spacers.” In variousembodiments described herein, the implants may include spinous processsupport surfaces, indented portions or saddle portions spaced apart by adistance (a), which corresponds to a desired distance for distraction orspacing of two adjacent spinous processes. Other embodiments similarlyprovide a desired distance for distraction or spacing of two adjacentspinous processes. Depending on the material and/or design of theimplant, the desired distraction or spacing distance may vary somewhatafter insertion, for example if a patient moves its spine into aposition that causes further distraction. For example, in certainembodiments the implant may be resiliently compressible or expandable inthe cranial-caudal direction such that the implant may support and oradjust to dynamic movement of the spine. Although not depicted in thefigures discussed below, it is contemplated that embodiments of thepresent invention may be extended to provide distraction or spacing ofmore than two adjacent spinous processes.

Implants in accordance with the present invention may be attached to oneor more spinous processes or other portion of the spine, or may attachto itself in such a manner as to secure the implant between two adjacentspinal processes. By way of example, implants in accordance with thepresent invention may be attached to one or both spinous processes orother portion of the spine (see e.g., FIGS. 22-24) by one or more pins,screws, wires, cables, straps, surgical rope, sutures, elastic bands, orother fastening devices. Alternatively implants of the present inventionmay secure themselves in place without a fastening device attacheddirectly to a spinous process or other portion of the spine (see e.g.,FIGS. 19-21). “Securing” implants between spinous processes, does notrequire that the implant not move at all, but rather means that theimplant does not move so far away from between the spinous processesthat it does not perform the function of maintaining a desireddistraction distance or space between the adjacent spinous processes.

Implants in accordance with the present invention may be secured betweenspinous processes by methods other than using a fastening device. Forexample, according to certain embodiments, implants in accordance withthe present invention may be secured in place with respect to spinousprocesses by mechanical forces resulting from the design of the implant,including the shape itself. Exemplary implants may also be secured tospinous processes, by surface modifications to portions of the implant,such as to create frictional forces or other bonds between the implantand spinous processes. Such surface modifications may include mechanicalmodifications to the surface (see e.g., spikes in FIG. 16) and/or one ormore coatings. Such mechanical forces and/or surface modifications maybe utilized in addition to, or in place of various other attachmentmethods described herein.

Implants in accordance with the present invention may be made of one ormore materials suitable for implantation into the spine of a mammalianpatient. Materials in accordance with the present invention may bebiocompatible with a mammalian patient and/or may have one or moresurface coatings or treatments that allow the spacers to bebiocompatible. Materials in accordance with the present invention mayinclude one or more materials having sufficient load capability and/orstrength to maintain the desired spacing or distraction between spinousprocesses. Depending on the design employed, certain embodiments mayhave components or portions made of a material having certainflexibility, as desired for the particular application. Additionally,the materials of the present invention may be made of one or morematerials that maintain their composition and shape for as long a timeas possible without degrading or decomposing or changing shape, suchthat replacement of the implant is avoided.

Suitable materials for use in accordance with the present inventionwould be known to those skilled in the art. Non-limiting examplesinclude one or more materials selected from titanium,polyetheretherketone (PEEK), ceramics, deformable materials, bone,allograft, demineralized or partially demineralized bone, allograftligament, and polyurethane (for example, for portions of the insertwhere cushioning is desired). Similarly, any fastening devices may bemade of materials having one or more of the properties set forth withrespect to the implant itself. For example, screws or pins may includetitanium and straps may include polyethylene. In some embodiments,primarily radiolucent material may be used. In this regard, radio-opaquematerial or markers may be used in combination with the radiolucentmaterial to facilitate implantation. Exemplary radio-opaque materialincludes but is not limited to titanium alloys, tantalum or other knownradio-opaque marker material. As indicated above, implants in accordancewith the present invention may have one or more portions that may havemodified surfaces, surface coatings, and/or attachments to the surface,which may assist in maintaining the spacer in a desired position, forexample by friction. Suitable surface modifications, coatings, andattachment materials would be known to those skilled in the art, takinginto consideration the purpose for such modification, coating, and/orattachment.

Implants according to the present invention may be adapted to beinserted between a first and second spinous process at any region in thespine. Although typically implants according to the present inventionmay be inserted in the lumbar region, it is contemplated that it ispossible to configure inserts according to the present invention forinsertion into other regions such as for example, the thoracic orcervical region. In general, implants according to the invention mayhave varying profiles when viewed in a saggital plane. In this regard,the implants can have varied cross-sectional shapes to conform to thevaried anatomical shapes of the interspinous spaces of the spine.

Methods for Treating Stenosis and Methods of Inserting an Implant

Methods are provided for treating spinal stenosis. Methods are alsoprovided for inserting an implant. These methods may include implantinga device to create, increase, or maintain a desired amount ofdistraction, space, or distance between adjacent first and secondspinous processes. The adjacent first and second spinal processes may beaccessed by various methods known by practitioners skilled in the art,for example, by accessing the spinous processes from at least onelateral side/unilateral, bilateral, or midline posterior approach.

Certain methods of the present invention include creating an incision ina patient to be treated, removing/dilating any interspinous ligaments ina position in which the implant is to be placed in the patient, sizingthe space between adjacent spinous processes (for example using trials),and inserting an implant of the appropriate size between the adjacentspinous processes. Methods of the present invention may include securingthe implant to one or more of the spinous processes, to one or moreother portions of the patient's spine, and/or to itself such that theimplant maintains its position between the spinous processes.

Methods of the present invention may include dilating or distracting thespinous processes apart from one another before sizing and/or beforeinserting the implant. Methods may vary depending on which implant isbeing inserted into a patient. For example, certain implants may requiredistracting the spinous processes apart before inserting the implant,while other implants may themselves dilate or distract the spinousprocesses while inserting the implant. In embodiments where the implantsthemselves dilate or distract the spinous process, the implant may have,for example, a predetermined shape to dilate, distract, or otherwisemove or separate apart adjacent spinous processes such as a cam orcam-like profile, it may have a distraction device that is deployed,and/or it may have a tapered expander to distract an opening between theadjacent spinous processes or other features to facilitate distractionof the adjacent spinous processes.

According to certain embodiments, spacers may be placed between thespinous processes anterior to the supraspinous ligament, avoiding thenerves in the spinal canal. The procedure may be performed under localanesthesia. For surgical procedures, in which an implant is beinginserted into the lumbar region, the patient may be placed in the rightlateral decubitus position with the lumbar spine flexed.

According to certain embodiments, one or more probes may be used tolocate the space between the spinous processes. Depending on the designof the spacer to be inserted, the space may be widened, for example witha dilator before inserting the implant.

While the present invention is satisfied by embodiments in manydifferent forms, there will herein be described in detail embodiments ofthe invention, with the understanding that the present disclosure andexamples are to be considered as exemplary and/or illustrative of theprinciples of the invention and are not intended to limit the scope ofthe invention to the embodiments illustrated and described. As would beapparent to skilled artisans, various changes and modifications arepossible and are contemplated within the scope of the inventiondescribed, and may be made by persons skilled in the art withoutdeparture from the spirit of the invention.

Systems and Kits

Kits in accordance with the present invention may include one or moreimplants. For example, kits having at least one implant such as thosedepicted in FIGS. 1 a-1 d or 2, may include various sizes of implantshaving varying distances (a), for example incremental distances, such as2 mm increments.

Kits in accordance with the present invention may further include one ormore tools or other devices that may be useful in distracting spinousprocesses, and/or selecting, inserting, positioning, and/or securing oneor more implants. By way of non-limiting example, such tools and/ordevices may include one or more of the following: those adapted toremove/dilate interspinous ligaments in the way of inserting the implantinto the patient; those for sizing the space between adjacent spinousprocesses such as one or more trials of varying or various sizes (seee.g., the device depicted in FIG. 1 g); those for inserting an implantbetween adjacent spinous processes; those for distracting the spinousprocesses apart from one another; and those for securing one or moreimplants between adjacent spinous processes.

Tools or devices for distracting the spinous processes may be adaptedfor example, to provide for distraction in the range of about 5 mm toabout 15 mm. However, devices that can distract up to and above 22 mmmay be used depending on the characteristics of the patient.

Tools and devices that may be used to secure one or more implantsbetween spinous processes may include for example, one or more pins,screws, wires, cables, straps, surgical rope, sutures, or otherfastening devices, and/or tools for inserting, securing or tighteningsuch fastening devices. For example, a stapler such as that depicted inFIG. 1 f may be used in some embodiments to secure an implant such asthat depicted in FIGS. 1 a-1 e.

In a further aspect of the invention, systems may be provided thatinclude at least one implant and at least one fastening device. Systemsin accordance with the present invention may further include one or moreof the following: one or more tools or devices for removing anyinterspinous ligaments in the way of inserting the implant; one or moretools or devices for sizing the space between adjacent spinousprocesses; and one or more tools or devices for distracting spinousprocesses, and/or selecting, inserting, positioning, and/or securing oneor more implants.

Further non-limiting examples of implants, methods, kits and systems inaccordance with the present invention are set forth below with respectto the described implant embodiments.

Referring now to FIGS. 1 a-1 e, one exemplary embodiment of an implant 1according to the invention is shown for creating, increasing, ormaintaining distraction between adjacent spinous processes. In general,implant 1 is adapted and configured to be placed between adjacentspinous processes. For example, referring to FIGS. 1 d and 1 e, a sideview of implant 1 is shown in implanted positions in relation to twoadjacent spinous processes 5 between which the implant is implanted. Asbest seen in FIGS. 1 a-1 c, implant 1 is a unitary body with a generaloval, ovoid, oblong, football-like shape and generally includes at leastone rounded lateral side surface or portion 2, and two or more indentedportions, troughs, or saddle portions 3 adjacent the longitudinal ends.In one embodiment, implant 1 comprises two rounded lateral side surfacesor portions 2. Saddle portions 3 are generally configured anddimensioned to engage the spinous processes 5 and each generallyincludes a saddle surface 4 with tines or walls 6 extendinglongitudinally beyond the lateral sides thereof. Saddle surfaces 4 arespaced longitudinally apart by a distance (a), which generallycorresponds to the desired distance for distraction or spacing of twoadjacent spinous processes 5. Implant 1 has a maximum lateral width (b)measured between the outermost point or section of the lateral sidesurfaces or portions 2. The distance (a) may vary with respect todistance (b) and in a preferred embodiment distance (a) is greater thandistance (b). According to certain embodiments distance (a) may beproportional to distance (b). Non-limiting examples of distance (a) mayinclude any distance from about 3 mm to about 25 mm or from about 7 mmto about 21 mm.

Walls 6 are generally spaced in the lateral direction a sufficientdistance to accommodate the width of a spinous process therebetween andwalls 6 may contact or engage the lateral sides of the spinous processwhen the implant is implanted. In this regard, walls 6 generally preventor limit lateral movement of the implant when the implant is implanted,such as for example when in the position shown in FIG. 1 e.

In certain variations of the present embodiment, implant 1 may beattached to one or both of the adjacent spinous processes to secure theimplant. By way of non-limiting example, the implant may have openings8, which permit the attachment of the implant to one or both spinousprocesses by one or more fastening devices. As discussed above,according to certain embodiments, implants in accordance with thepresent invention may be secured in place with respect to spinousprocesses by mechanical forces resulting from the design of the implant,including the shape itself. In other embodiments, implant 1 may also besecured to spinous processes, by surface modifications to portions ofthe implant, such as modifications to the inner surfaces of walls 6 tocreate frictional forces or other bonds between the implant and spinousprocesses. Such surface modifications may include mechanicalmodifications to the surface and/or one or more coatings. Suchmechanical forces and/or surface modifications may be utilized inaddition to, or in place of (in which case, the implant may have noopenings 8) various other attachment methods described herein.

FIG. 2 exemplifies another implant 10 according to the present inventionadapted to be placed between adjacent spinous processes. Implant 10comprises at least one rounded lateral side surface or portion 12, andtwo or more indented portions, troughs, or saddle portions 3. Implant 10of FIG. 2 is similar to implant 1 of FIG. 1, except that the lateralside surface(s) or rounded portion(s) 12 may include one or moreportions 16 that modify the curve of the rounded portion(s) 12. In thisembodiment, portion 16 reflects a concave section positioned betweenconvex sections of rounded portion(s) 12. In alternate embodiments,lateral side surfaces or portions 12 may have differing shapes otherthan simple curves that may facilitate rotation in situ and/or provideadditional mechanical advantage to distract the spinous processes inoperation. Similar to implant 1, the saddle portions 3 are spaced apartby a distance (a), which generally corresponds to the desired distancefor distraction or spacing of two adjacent spinous processes.

According to methods of the present invention, implants 1, 10 may beinserted between two adjacent spinous processes 5 wherein a portion ofat least one rounded portion 2, 12 may contact at least one of theadjacent spinous processes as shown, for example in FIG. 1 d for implant1, and the implant may be rotated until the two adjacent spinousprocesses are positioned into the saddle portions 3 of the implant, asshown in FIG. 1 e.

The implant itself may serve to dilate or distract the spinous processesas it is being inserted and/or after insertion. For example, inembodiments in which the implant is similar to that depicted in FIGS. 1and 2, the implant may be initially inserted laterally between thecompressed adjacent spinous processes as shown in FIG. 1 d. Thesupraspinous ligament may or may not be removed. In an initialpre-implantation condition, the adjacent spinous process may becompressed such that the initial space or longitudinal distance betweenthe processes may be equal to or smaller than distance (b) of implant 1.During lateral insertion of the implant, one or more lateral sidesurfaces or portions 2, 12 of the implant may contact one or both of thespinous processes 5 and may initially distract the processes a distance(b). As the implant is inserted further between the spinous processesand rotated, the rounded portion(s) may distract the spinous processesfurther apart from one another, until the implant is rotated into alongitudinal or implanted position and the spinous processes are fittedinto the saddle portions 3 of the implant. In operation, lateral sidesurfaces or portions 2, 12 of implants 1, 10 engage the adjacent spinousprocesses as the implant is rotated to act or perform in a cam-likemanner to translate the rotational force to separate the spinousprocesses in the longitudinal or cranial-caudal direction as the implantis rotated. In one embodiment, implants 1, 10 may be rotated about 90degrees or from the horizontal or lateral position to the vertical orlongitudinal position. The maximum distraction of spinous processes bythe implant is distance (c) depicted in FIG. 1 a. Once the implant isimplanted and after the spinous processes are fitted into the saddleportions 3 of the implant, the implant may maintain the spinousprocesses in a distracted or spaced condition, for example where thedistance (a) of the implant is greater than a pre-implantation distancebetween the spinous processes.

Kits having at least one implant such as those depicted in FIGS. 1 and2, may include various sizes of implants having varying distances (a),for example incremental distances, such as 2 mm increments.

Tools and devices that may be used to secure one or more implantsbetween spinous processes may include for example, one or more pins,screws, wires, cables, straps, surgical rope, sutures, or otherfastening devices, and/or tools for inserting, securing or tighteningsuch fastening devices. For example, a staple device 7 such as thatdepicted in FIG. 1 f may be used to secure an implant such as thosedepicted in FIGS. 1 a-1 e. Staple device 7 may be used to crimp theimplant in place, create holes in the spinous process in alignment withopenings 8 to facilitate insertion of alternate fastening devices,and/or clasp the implant to the spinous process and remain in-situ. Thefollowing is a non-limiting example of how such a staple device may beused. Pins, screws or other fastening devices 9 at the open ends 11 ofthe staple device may be aligned adjacent to the openings 8 of theimplant on either side of a spinous process after the implant ispositioned with respect to the spinous processes. The open ends 11 ofthe staple device are then compressed together such that the fasteningdevices 9 secure the implant to the spinous process through openings 8of the implant.

Referring to FIGS. 3 a-3 c, additional embodiments of implants accordingto the present invention adapted to be placed between adjacent spinousprocesses are shown. Implants 30, 32, and 34 generally comprise at leastone substantially straight lateral side surface or portion 36, and twoor more indented portions, troughs, or saddle portions 3 adjacent thelongitudinal ends. Each of the straight side portions 36 may includeproximal ends 37 and distal ends 38 that are rounded such as shown inFIG. 3 c with respect to implant 32, or squared such as shown in FIG. 3a with respect to implant 30. In embodiments having more than onestraight portion 36, in one variation at least two of the straightportions may be substantially parallel to one another, such as shown inFIG. 3 a with respect to implant 30. In alternative embodiments, the atleast two straight portions 36 may not be substantially parallel, suchas shown in FIG. 3 b with respect to implant 32 where proximal ends 37of straight portions 36 are spaced laterally closer together than thecorresponding distal ends 38 of the straight portions 36, creating atapered configuration.

As with previous embodiments, the saddle portions 3 are spacedlongitudinally apart by a distance (a), which may vary as describedherein with respect to other embodiments of the invention. As withprevious embodiments, walls 6 of saddle portions 3 may be spacedlaterally apart a sufficient distance to allow the spinous processes tofit within the saddle portions 3. Walls 6 may also be close enoughtogether such that when the implants are positioned such that thespinous processes are within saddle portions 3, the implant may beattached to one or both of the adjacent spinous processes. By way ofexample, the implant may have openings 8, which allow one to attach theimplant to one or both spinous processes by one or more fasteningdevices or methods as described herein.

According to methods of the present invention, the implant may beinserted between two adjacent spinous processes and the implant may berotated until the two adjacent spinous processes are positioned into thesaddle portions 3 of the implant. Certain methods of the presentinvention include creating an incision in a patient to be treated,removing any spinous ligaments in a position in which the implant is tobe placed in the patient, sizing the space between adjacent spinousprocesses (for example using trial blocks or spacers), and inserting animplant of the appropriate size between the adjacent spinous processes.Methods of the present invention may include distracting the spinousprocesses apart from one another before sizing and/or before insertingthe implant. Methods of the present invention may include securing theimplant to one or more of the spinous processes and/or to one or moreother portions of the patient's spine, such that the implant maintainsits position between the spinous processes.

The implant itself may serve to distract the spinous processes as it isbeing inserted and/or after insertion. For example, implant 32 of FIG. 3b may be inserted with the narrow or tapered end (where the ends 37 ofsides 36 are laterally closer together) first. In operation, as theimplant is further inserted between the spinous processes, theincreasing distance between sides 36 may serve to distract the spinousprocesses from one another.

Referring to FIGS. 4 a-4 b, another embodiment of an implant 40 adaptedto be placed between adjacent spinous processes is shown. Implant 40generally comprises an oblong body and includes a narrow end 42 and awide end 43 to form a wedge-like shape.

According to methods of the present invention, the implant may beinserted between two adjacent spinous processes such that the narrow end42 is inserted first and the wedge-like shape serves to distract thespinous processes as the implant is further inserted between the spinousprocesses.

Referring to FIGS. 5-8, additional embodiments of implants according tothe invention for creating, increasing, or maintaining distractionbetween adjacent spinous processes are shown. In particular, FIGS. 5-8exemplify implants adapted to be placed between adjacent spinousprocesses, which generally include a main body 54 and at least two arms56. In general, the implants may be resiliently compressible orexpandable such that the implants may support and or adjust to dynamicmovement of the spine. In this regard, the implants may include one ormore biasing members or springs 58 or other configurations or materialsthat allow the body to dynamically distract less or more distance.

Referring to FIG. 5 one exemplary embodiment of an implant 50 is shownwherein the entire device is positioned between the spinous processes.In this regard, arms 56 of implant 50 are configured to contact,support, or otherwise engage the respective superior and inferiorsurfaces of the adjacent spinous process without contact with thelateral or side surfaces of the spinous processes: In this embodiment,implant 50 may be attached directly or secured to the superior andinferior surfaces or the spinous processes for example by one or morefastening devices 57, such as screws, as shown in FIG. 5. Biasing memberor spring 58 permits arms 56 of implant 50 to resiliently compresstogether or expand apart in the cranial-caudal direction. In thisregard, spring 58 provides dynamic support between the adjacent spinousprocesses and accommodates extension and flexion of the spine.

Referring to FIGS. 6 a and 6 b, another embodiment of an implant 60 ofthe present invention is shown. Implant 60 is similar to implant 50described above, except the arms 56 or portions thereof are not entirelypositioned between the spinous processes. In this embodiment, the arms56 of implant 60 may be attached for example, to the sides of thespinous processes 5 by one or more fastening devices 57, such as screws,as depicted in FIG. 6 a.

As best seen in FIG. 6 b, implant 60 may include saddle portions 3 whichinclude arms or walls 6. As depicted in FIG. 6 b, in one embodimentimplant 60 may have at least one saddle portion 3. Arms or walls 6 maybe spaced laterally apart a sufficient distance to allow the spinousprocesses 5 to fit within the saddle portions 3. Arms or walls 6 mayalso be close enough together such that when the implants are positionedsuch that the spinous processes are within saddle portions 3, theimplant may be attached to one or both of the adjacent spinous processesas discussed above and/or secured in place by virtue of its design.

FIGS. 7 and 8 depict embodiments similar to those shown in FIG. 5 wherethe entire device is positioned between the spinous processes. Theembodiments of FIGS. 7 and 8 may be attached to the spinous processesfor example by one or more fastening devices 72, as shown in FIGS. 7 and8. Fastening device 72 may be attached to an arm 56 of the implant and aspinous process 5. Optionally, a strap 74 or other fastening device maybe used to further secure the implant to one or both spinous processes.

Referring to FIG. 9, another exemplary embodiment of an implant 90according to the present invention is shown. Implant 90 generallycomprises a distal or first end 91 having a first shaft 92 extendingproximally therefrom and a proximal or second end 93 with a second shaft94 extending distally therefrom. A spring 96 is positioned concentric toshaft 92 and configured and dimensioned to fit coaxially inside asubstantially cylindrical opening of the second shaft 94 of second end93. The configuration may allow implant 90 to be somewhat flexible afterimplantation between spinal processes, by virtue of the spring 96, whichallows first end 91 and second end 93 to move further apart and closertogether with respect to each other after implantation into the patient.Similar to previously described embodiments, spring 96 provides dynamicsupport between the adjacent spinous processes and accommodatesextension and flexion of the spine.

According to other embodiments, the spring configuration facilitatesimplantation into the patient as it allows the first end 91 and secondend 93 to be compressed together during implantation and released,similar to, for example, a pen-spring. In this regard, a surgeon orother operator of the device may position the spinous processes insaddle portions 3 of the first and second ends 91, 93, more easily.

In certain embodiment, implant 90 may be secured in position between thespinous processes for example, by one or more screws or pins 97 and/orby one or more straps 98 positioned around one or both spinousprocesses.

Referring to FIG. 10 another implant 100 according to the invention isshown. Implant 100 generally comprises a first portion 101 and a secondportion 103. One or both portions may have a threaded connection orturnbuckle 104 that threadedly connects the first and second portionstogether. Implant 100 may be expanded or contracted in thecranial-caudal or longitudinal direction by rotating tumbuckle(s) 104.In this regard, implant 100 may be adjusted after implantation betweenspinal processes, by virtue of the threaded connection between the firstand second portions 101, 103, which allow the first and second portionsto move further apart and closer together with respect to each otherafter implant 100 is inserted into the patient. In this regard, implant100 may be used to distract the adjacent spinous processes in situwithout the need for an additional distraction tool. Similar to previousembodiments, implant 100 may be secured in position between the spinousprocesses for example, by one or more screws or pins and/or by one ormore straps 106 that wrap around one or both spinous processes. Both ofthe first and second portions of implant 100 may be inserted between thespinous processes substantially simultaneously, or one portion may beinserted followed by the other portion.

Referring to FIG. 11, another embodiment of an implant 110 according tothe present invention is shown. In general, implant 110 may beresiliently compressible or expandable such that the implant may supportand or adjust to dynamic movement of the spine. As seen in FIG. 11,implant 110 is shown in relation to two adjacent spinous processes 5between which the implant is implanted. Implant 110 generally comprisesa main body 111 having at least one top end 112 and at least one bottomend 113, a first posterior side 114 extending between the top and bottomend, and a second anterior side 115 extending from the top end 112 tobottom end 113. At least a portion of each of the first and second sides114, 115 is curved. In some embodiments, at least one of the first andsecond sides 114, 115 is curved in a convex direction (e.g. second side115 in FIG. 11) and at least one of the first and second sides 114, 115is curved in a concave direction (e.g. the first side 114 in FIG. 11).In operation, the curved configuration may function similar to a biasingmember or spring such that implant 110 may be flexible or resilientlycompressed or expanded in the cranial-caudal direction. Optionally, themain body 111 may contain one or more openings 116. Opening(s) 116 mayoptionally be curved similar to the convex and concave directions of thefirst and second sides 114, 115 of the body as depicted in FIG. 11, andmay provide or enhance flexibility of the implant. The material(s) fromwhich the implant is made may also provide or enhance flexibility of theimplant. For example, implant 110 may be made from a resilientlydeformable material such that the implant may be resilientlycompressible or expandable to support and or adjust to dynamic movementof the spine. In this regard, the shape and configuration of the implantmay allow the implant to resiliently deform in the cranial-caudaldirection and provide dynamic support between the adjacent spinousprocesses to accommodate extension and flexion of the spine.

Embodiments according to the present invention may be positioned orimplanted such that the body 111 is entirely between two spinousprocesses 5, or as depicted in FIG. 11, one or both of the top 112 andbottom 113 ends of the body may overlap one or more sides of one or moreof the spinous processes. In embodiments where one or both of the topand bottom ends overlap to the one or more of the sides of one or moreof the spinous processes, the body 111 may have two top ends 112 (one oneither side of a spinous process) and two bottom ends 113 (one on eitherside of a spinous process). Alternatively, the top and bottom ends ofthe implant may overlap with the spinous processes on the same side, ora second implant may optionally be implanted on the opposite side of thespinous processes. In certain embodiments, implant 110 may be secured inplace by the methods described herein, which may include for example,connecting implant 110 to the spinous process through holes 8 in theimplant.

Referring to FIG. 12, another embodiment of an implant 120 according tothe present invention is shown in relation to two adjacent spinousprocesses 5 between which the implant is implanted. In general, implant120 may allow dynamic relative movement between adjacent spinousprocesses. Implant 120 is adapted and configured to be placed betweenadjacent spinous processes, and generally includes a top body 127 and abottom body 128 rotatably interconnected at a rotation body 129. The topbody and bottom body may be of any formation so long as they can rotateas desired about the rotation body as desired for implantation and/orfor flexion purposes after implantation. The rotation body may be forexample, a ball and socket configuration. For example, the ball andsocket configuration may allow implant 120 adjust to dynamic movement ofthe spine once the implant is inserted. In this regard, implant 120 mayaccommodate limited contraction and expansion of adjacent spinousprocesses in the cranial-caudal direction as well as relative movementin the medial-lateral direction and posterior-anterior direction toaccommodate dynamic movement of the spine. In the cranial-caudaldirection, implant 120 may have a maximum distraction distance (d) tosupport limited flexion of the spine.

According to certain embodiments of the present invention one or both ofthe top and bottom bodies may overlap to the side of the spinousprocess. According to these embodiments, the top body 127 and/or thebottom body 128 may overlap on either side of a spinous process.Alternatively, the top body 127 and bottom body 128 overlap with thespinous processes on the same side, and a second implant may beoptionally implanted on the opposite side of the spinous processes. Inother embodiments, implant 120 may include saddle portions as describedpreviously.

According to methods of the present invention, the implant may beinserted between two adjacent spinous processes 5, where the top body127 and/or the bottom body 128 are rotated about the rotation body 129(either towards or away from each other), such that the height (d) ofthe implant is not at its maximum. After the implant is positionedbetween spinous processes, the top body 127 and/or bottom body 128 maybe rotated with respect to the rotation body 129 until the implant ispositioned at a desired height (d). The implant may be locked or securedto the desired height or adapted to allow a certain flexibility orrotation about the rotation body 129. In certain embodiments, implant120 may be secured in place by the methods described herein, which mayinclude for example, connecting implant 120 to the spinous processthrough holes 8 in the implant.

FIGS. 13 a-b depict another embodiment of an implant 130 according tothe present invention in relation to two adjacent spinous processes 5between which the implant is implanted. Similar to implant 110 describedwith respect to FIG. 11, implant 130 may be resiliently compressible orexpandable such that the implant may support and or adjust to dynamicmovement of the spine. As seen in FIG. 13 a, implant 130 generallyincludes a body 131 having a top end 132 and a bottom end 133, a firstside 134 extending between the top and bottom end, and a second side 135extending from the top to bottom end, where at least a portion of eachof the first and second sides are curved. FIG. 13 depicts embodimentswhere at least one of the first and second sides has a portion curved ina convex direction and at least one of the first and second sides has aportion curved in a concave direction. In operation, the curvedconfiguration may function similar to a biasing member or spring suchthat implant 130 may be flexible or resiliently compressed or expandedin the cranial-caudal direction. The material(s) from which the implantis made may also provide or enhance flexibility of the implant. Forexample, implant 130 may be made from a resiliently deformable materialsuch that the implant may be resiliently compressible or expandable tosupport and or adjust to dynamic movement of the spine. In this regard,the shape and configuration of the implant may allow the implant toresiliently deform in the cranial-caudal direction and provide dynamicsupport between the adjacent spinous processes to accommodate extensionand flexion of the spine.

Embodiments according to the present invention may comprise body 131positioned entirely between the spinous processes, or as depicted inFIG. 13, one or both of the top 132 and bottom 133 ends of the body 131may overlap to the side of the spinous process. In embodiments where oneor both of the top and bottom ends overlaps to the side of the spinousprocess body 131 may have saddle portions 3 on the top and bottom endsof implant 130 wherein each saddle includes lateral saddle walls 6 (oneon either side of a spinous process). A non-limiting example of such anembodiment is depicted in FIG. 13 b, depicting two top saddle walls 6 oneither side of a spinous process, and two bottom saddle walls 6 oneither side of a spinous process. In an alternative embodiment, the topend 132 and bottom end 133 of implant 130 may overlap the spinousprocesses on the same side of the spinous process, and a second implantmay be optionally implanted on the opposite side of the spinousprocesses. Implant 130 may be secured in place by any suitable methodsdescribed herein.

Referring to FIGS. 14 a-b, another embodiment of an implant 140according to the present invention is shown in relation to two adjacentspinous processes 5 between which the implant is implanted. Implant 140is configured and adapted to be placed between adjacent spinousprocesses, and generally comprises a body 145 and a securing device 146.The body 145 is positioned between the spinous processes 5. The securingdevice 146 weaves through both the body 145 and the spinous processes(for example, as depicted in the front view FIG. 14 b) to maintain thebody's position between the spinous processes. The securing device 146may have a coupling device 147 to tighten securing device 146 orotherwise add tension to the device to secure implant 140 in position.

The body 145 may be of any desirable shape or size such that it fitsbetween the spinous processes, optionally, with portions thereofoverlapping to the sides of the spinous processes (as depicted forexample in FIG. 14 b). The body needn't contact either spinous processat any particular time, but may allow for space between the spinousprocess 5 and the body 145. The body 145 may be made of any suitablematerial, but according to certain embodiments, the body 145 is morerigid than the securing device 146.

The securing device 146 may be in one or more pieces, components, and/ormaterials. Securing device 146 may pass through the body at one or morepositions and through the spinous processes, at one or more positions,so long as the body is generally maintained between the spinousprocesses.

Referring to FIGS. 15 a-b, another embodiment of an implant 150according to the present invention is shown in relation to two adjacentspinous processes 5 between which the implant is implanted. Implant 150is configured and adapted to be placed between adjacent spinousprocesses, and generally comprises a top body 151 and a bottom body 152rotatably and/or linkingly connected. The top body 151 may have either amale or female fitting portion, and the bottom body 152 may have acorresponding opposite fitting portion. According to one embodimentshown in FIG. 15 a, the top body 151 has a female fitting portion 153,and the bottom portion has a male fitting portion 154. The fittingportions may be of any configuration so long as they fit together.Similarly, the top body and bottom body may be of any formation so longas they fit together at the male/female portions. The male and femaleportions may optionally be attached to one another. Further the male andfemale portions may optionally be attached such that the top portion andbottom portion can rotate as desired about an attachment position forimplantation purposes and/or for flexion purposes after implantation.The male and female portions may be for example, a tongue and grooveconfiguration. For example, the tongue and groove configuration mayallow implant 150 adjust to dynamic movement of the spine once theimplant is inserted. In this regard, implant 150 may accommodate limitedcontraction and expansion of adjacent spinous processes in thecranial-caudal direction as well as relative movement in theposterior-anterior direction to accommodate dynamic movement of thespine.

According to certain embodiments of the present invention one or both ofthe top and bottom bodies may overlap to the side of the spinous processas depicted in FIG. 15 a. According to these embodiments, the top body151 and/or the bottom body 152 may overlap on both sides of a spinousprocess (as shown for example, in FIG. 15 b). In embodiments where oneor both of the top and bottom ends overlaps to the side of the spinousprocess, top and bottom bodies 151, 152 may have saddle portions 3 onthe top and bottom ends of implant 150 wherein each saddle portionincludes lateral saddle walls 6 (one on either side of a spinousprocess). A non-limiting example of such an embodiment is depicted inFIG. 15 b, depicting two top saddle walls 6 on either side of a spinousprocess, and two bottom saddle walls 6 on either side of a spinousprocess. In an alternative embodiment, the top end 151 and bottom end152 of implant 150 may overlap the spinous processes on the same side ofthe spinous process, and a second implant may be optionally implanted onthe opposite side of the spinous processes. Implant 150 may be securedin place by any suitable methods described herein.

Referring to FIGS. 16-18, additional embodiments of implants 160, 170,180 according to the present invention are shown. Implants 160, 170, and180 may allow dynamic relative movement between adjacent spinousprocesses and generally include a top U-shaped body 163 configured tomovingly engage a bottom U-shaped body 164. Each U-shaped body has anopen end 167 and a closed end 168. The open ends 167 of the U-shapedbodies are configured such that spinous processes may fit within a spacecreated thereby. The closed ends 168 of the U-shaped bodies aregenerally configured to be directed toward one another afterimplantation. The top and bottom U-shaped bodies may be directly orindirectly engaged to one another or they may simply contact one anotherdirectly or indirectly. For example, the top and bottom U-shaped bodiesmay be configured such that the closed ends 168 fit together directly asdepicted in FIG. 18 and may include one ore more indented portions 165to mate or fit with an adjacent U-shaped body. The U-shaped bodies maymovingly engage one another similar to a ball and socket configuration.In this regard, implants 160, 170, and 180 may adjust to dynamicmovement of the spine once the implant is inserted. For example, theimplants may accommodate limited contraction and expansion of adjacentspinous processes in the cranial-caudal direction as well as relativemovement in the medial-lateral direction and posterior-anteriordirection to accommodate dynamic movement of the spine. In thecranial-caudal direction, the implants may have a minimum distractiondistance to support limited extension of the spine.

Indirect contact or attachment may occur for example, in embodimentswhere there are one or more intermediate bodies, such as intermediatebody 172 of FIG. 17. The intermediate body 172 may be of anyconfiguration that fits at least partially between the top and bottomU-shaped portions after insertion of the implant. According to certainembodiments, the intermediate body may be shaped such that it configuresto the shape of the top and/or bottom U-shaped bodies. For example, inFIG. 17, the intermediate body 172 is shaped to fit within indentedportions 165 provided in the top and bottom U-shaped bodies. Theintermediate body 172 may be made of any material suitable forimplantation into a mammalian patient and may be selected based on thedesired function of the intermediate body. For example, the intermediatebody 172 may be made of a polymer material that may be resilientlycompressible in the cranial-caudal direction.

Implants in accordance with the present embodiments may be secured inplace by the methods described herein, which may include for example,connecting the implant to the spinous process through holes 8 in theimplant as depicted for example in FIG. 18. Exemplary implants may besecured to spinous processes, by surface modifications to portions ofthe implant, such as modifications to surfaces of an inside surface 169of the U-shaped bodies. Such surface modifications may includemechanical modifications to the surface (see e.g., ridges 171 in FIG.16) and/or one or more coatings. Such mechanical forces and/or surfacemodifications may be utilized in addition to, or in place of variousother attachment methods described herein.

According to certain methods of the present invention the top U-shapedportion 163 and the bottom U-shaped portion 164 may be inserted betweentwo adjacent spinous processes together or separately. By way ofnon-limiting example, embodiments such as those depicted in FIG. 16 maybe inserted by a straight posterior insertion, or they may be insertedby positioning one U-shaped portion over a spinous process andthereafter rotating the other U-shaped portion over the other spinousprocess. Any intermediate bodies may be inserted before, substantiallysimultaneously with, or after insertion of the top and bottom U-shapedportions.

Referring to FIGS. 19-21, additional embodiments of the invention forcreating, increasing, or maintaining distraction between adjacentspinous processes are shown. Implants 190, 200, and 210 depicted inFIGS. 19-21 generally include a first body 191 having a male portion 193and a second body 192 having a female portion 194, wherein the maleportion fits partially within the female portion. Upon inserting themale portion into the female portion, spaces are created above and belowportions of the male portion that are not within the female portion.Adjacent spinous processes may fit within those spaces and a minimumdistraction distance or space may be provided by the male portion.

The male portion 193 may be part of the first body 191 (as depicted inFIG. 19) or it may be one or more portions attached to the first body191 (as depicted in FIG. 21). The male portion 193 may be curved ortapered as depicted in FIG. 20 such that the further it is inserted intothe female portion, the greater the distraction between spinousprocesses.

Methods of the present invention may include the following: inserting afirst body 191 and a second body 192 of the implant on either side oftwo adjacent spinous processes; fitting the bodies together by insertinga male portion 193 of the first body 191 into a female portion 194 ofthe second body 192; and adjusting a depth of insertion to a desireddepth depending for example, on the size of spinous processes, and/orthe desired amount of distraction between the spinous processes. Methodsof the present invention may further include securing the implantbetween adjacent spinous processes.

Implants in accordance with the present embodiments may be secured bythe methods described herein. According to certain embodiments, thefirst body 191 and the second body 192 may be attached to one another,for example, by a pin 195, screw or other fastening device afterinsertion into a patient to secure the implant in position. Otherfastening devices or methods may be used in place of or in addition toattaching the first body 191 to the second body 192 for example, byconnecting the implant to one or both spinous processes or otherportion(s) of the spine.

Referring to FIGS. 22-24 additional embodiments of the invention forcreating, increasing, or maintaining distraction between adjacentspinous processes are shown, wherein the implants are not directlyattached to either spinous process, but are attached to other portionsof the spine 222.

As shown in FIG. 22, one embodiment of an implant 220 may include atleast two stabilization devices 227, which attach to a portion of thespine 222 and a distraction device 228, which maintains a spinousprocess 5 in a desired position or range of positions with respect tothe portions of the spine to which the stabilization devices 227 areattached. In one embodiment, distraction device 228 is an arcuate memberthat extends between the stabilization devices 227 and is configured toengage a portion of an adjacent spinous process. The stabilizationdevices 227 may be for example, screws. The distraction device 228 maybe for example, a polymer material and may be more flexible or resilientthan the stabilization devices 227. In general, implant 220 may allowdynamic relative movement between adjacent spinous processes. Inoperation, the curved configuration may function similar to a biasingmember or spring such that implant 220 may be flexible or resilientlycompressed in the cranial-caudal direction to support and or adjust todynamic movement of the spine. In this regard, the shape andconfiguration of the implant may allow the implant to resiliently deformin the cranial-caudal direction and provide dynamic support between theadjacent spinous processes to accommodate extension and flexion of thespine.

As shown in FIG. 23, one embodiment of an implant 230 may be attached toat least two non-spinous process portions of the spine 222. Implant 230generally comprises a zig-zag-shaped configuration, but embodimentsaccording to the present invention are not limited to suchconfigurations. Embodiments may include any formation and/or be made ofany material that provides a desired shape and degree of flexibility. Inalternate embodiments, implants may be configured such that they do ordo not contact one or both spinous processes upon insertion. Implant 230may contact one or both spinous processes after insertion based onmovement of the patient and/or movement of the spine. In operation, thezig-zag or curved configuration may function similar to a biasing memberor spring such that implant 230 may be flexible or resilientlycompressed or expanded in the cranial-caudal direction. The material(s)from which the implant is made may also provide or enhance flexibilityof the implant. For example, implant 230 may be made from a resilientlydeformable material such that the implant may be resilientlycompressible or expandable to support and or adjust to dynamic movementof the spine. In this regard, the shape and configuration of the implantmay allow the implant to resiliently deform in the cranial-caudaldirection and provide dynamic support between the adjacent spinousprocesses to accommodate extension and flexion of the spine.

As shown in FIG. 24 one embodiment of an implant 240 generally comprisesa main body 241 attached to at least one attachment device 242. Theattachment device 242 may be attached to at least two non-spinousprocess portions of the spine 222. In one variation of the embodimentdepicted in FIG. 24, attachment devices 242 may have a foldingconfiguration, which may assist in insertion and/or in flexibility ormovement of the implant 240 after insertion.

Implant bodies 241 may be in any configuration. According to certainembodiments, implant body 241 may include rigid material(s) and theattachment device 242 may be either rigid or at least partially flexibleor maneuverable. In certain embodiments, implant body 241 may beconfigured such that it may or may not contact one or both spinousprocesses upon insertion. For example, in certain variations, implantbody 241 may contact one or both spinous processes after insertion basedon movement of the patient and/or movement of the spine.

Referring to FIGS. 25-26, additional embodiments of implants accordingto the invention are shown for creating, increasing, or maintainingdistraction between adjacent spinous processes. Implants 250 generallyinclude a body 252 and one or more straps 253. The strap(s) 253 areconfigured such that they wrap around one or both spinous processes, andcan maintain the position of the body 252 with respect to the spinousprocesses. Maintaining the position of the body 252 with respect to thespinous processes, does not require that the body not move at all, butrather means that the body does not move so far away from between thespinous processes that it does not perform the function of maintaining adistraction between the spinous processes.

Referring to FIGS. 27 a-b, another embodiment of an implant 270according to the invention is shown for creating, increasing, ormaintaining distraction between adjacent spinous processes. Implant 270generally comprises a center body 274 having at least two male portions276, and at least two outside bodies 275 having at least two femaleportions 277. The male and female portions fit together to define a topspace above the center body 274, and a bottom space below the centerbody 274. Two adjacent spinous processes fit within the top and bottomspaces. The center and outside bodies, and the male and female portionsmay be of any configuration that defines adequate top and bottom spacesin which to fit the spinous processes. According to certain embodiments,the center body 274 is made of a softer material than the outside bodies275.

As shown in FIG. 27 b, the male portions 276 may be ribbed. Ribbing mayassist in maintaining the male portions 276 within the female portions277.

Methods of the present invention may include the following: inserting acenter body 274 between two adjacent spinous processes and inserting atleast two outside bodies on either side of the adjacent spinousprocesses; fitting the bodies together by inserting the male portions276 of the center body 274 into the female portions 277 of the outsidebodies 275; and adjusting a depth of insertion of the male portions intothe female portions to a desired depth depending for example, on thesize of spinous processes, and/or the desired amount of distractionbetween the spinous processes. Methods of the present invention mayfurther include securing the implant between adjacent spinous processes.

Implants in accordance with the present embodiments may be secured bythe methods described herein. According to certain embodiments, thecenter body 274 and one or both of the outside bodies 275 may beattached to one another, for example, by a pin, screw or other fasteningdevice after insertion into a patient to secure the implant in position.Other fastening devices or methods may be used in place of or inaddition to attaching the center body 274 to one or both outside bodies275, for example, by connecting the implant to one or both spinousprocesses or other portion(s) of the spine.

Referring to FIGS. 28-33, another embodiment of an implant 300 accordingto the present invention is shown for creating, increasing, ormaintaining distraction between adjacent spinous processes. Implant 300is adapted and configured to be placed between adjacent spinousprocesses. As shown in FIG. 28, implant 300 is generally H-shaped oranvil shaped with a saddle portion or central support portion 302extending laterally along axis 303 between lateral end portions 304,306. Support portion 302 comprises a top or proximal support surface 308and a bottom or distal support surface 310 spaced longitudinally apartby a height or distance 312, which generally corresponds to the desiredor predetermined distance for distraction or spacing of two adjacentspinous processes. As best seen on FIG. 28, in one embodiment, endportions 304, 306 partially protrude beyond the front and back surfaces309, 311 of support portion 302 thereby creating a slight indentationalong the front and back or anterior and posterior of central portion302. As described in more detail below, when implant 300 is insertedlaterally between adjacent spinous processes, the processes areinitially dilated a distance slightly greater than the depth 314 ofcentral portion 302. In this regard, in a first implantation positionthe spinous processes settle or center adjacent the indented region ofcentral support portion 302, as shown for example in FIG. 40. Inaddition, when implant 300 is in a second implantation position, asshown in FIGS. 41-42, the indentations on the front and back areconfigured and dimensioned to avoid contact with the dura.

End portions 304, 306 extend generally perpendicular to support portion302 and generally extend longitudinally beyond support surfaces 308, 310and generally form wing-like structures on the lateral ends of implant300. End portion 304 extends longitudinally along axis 305 and endportion 306 extends longitudinally along axis 307. In one embodiment,axes 305 and 307 are generally perpendicular to axis 303. In anotherembodiment, axes 303, 305, and 307 are coplanar. End portions 304, 306are spaced laterally apart by a width distance 315, which generallycorresponds to the desired or predetermined distance for accommodatingthe width of the spinous processes. The inner surfaces or walls of endportions 304, 306 may contact or engage the lateral sides of the spinousprocesses when the implant is implanted. In this regard, end portions304, 306 are configured and dimensioned to generally prevent or limitlateral movement of the implant when the implant is implanted. In onevariation, the space between end portions 304, 306 may be angled towardthe center of implant to align the spinous processes with respect tocentral portion 302. According to one aspect of the present invention,multiple implants of varying widths 315 may be provided in a kit forappropriate selection and installation by a surgeon.

In one embodiment, end portion 304 generally comprises a cylindrical,bullet, anvil or horn shape extending longitudinally from a roundedbottom or distal end 316 to a narrower tip, nipple, or bull nose shapedtop or proximal end 318. As best seen when viewed from the front as inFIG. 29, in one embodiment, the outer lateral surface portion 320 of endportion 304 is curved laterally outward from bottom end 316 to a pointadjacent top end 318. In this regard, the curved aspect resembles a hornor boot and facilitates a combined lateral and rotational or pivotalinsertion between spinous processes as the curved profile providesclearance during in-situ rotation or pivoting about an axis extending inthe anterior-posterior direction through end portion 304 adjacent thebottom end 316. In operation, implant 300 may be pivoted about bottomend 316 during lateral insertion such that end portion 304 is rotatedfrom a lateral or horizontal position (shown in FIG. 39) to an uprightor longitudinal position (shown in FIG. 40). According to another aspectof an embodiment of the invention, a rounded or curved inner transition322 may be provided between inner lateral surface 324 of end portion 304and proximal support surface 308 of support portion 302. Referring toFIG. 33, in one embodiment end portion 304 may be tapered or increase inthickness along its length such that the proximal tip 318 is narrower orthinner than the base or bottom end 316 when viewed from the end. At itsthickest point, front surface portion 323 of end 304 is spaced from backsurface portion 325 of end 304 by a distance 327. In this regard, thetapered feature acts or performs in a cam-like manner to translate thelateral or pivotal force to separate the spinous processes in thelongitudinal or cranial-caudal direction as the implant is inserted. Inalternate embodiments, outer lateral surface or portion 320 of endportion 304 may have differing shapes or curves that may facilitatelateral and/or pivotal insertion and/or provide additional mechanicaladvantage to distract the spinous processes in operation.

Referring to FIG. 30, in one variation, support portion 302 has agenerally rectangular cross-section with a height 312 and a depth 314.In one embodiment, height 312 is greater than depth 314. In onevariation, height 312 is about 2 mm greater than depth 314. In alternateembodiments, any suitable range of heights and depths may be utilized.In one embodiment, a center locating pin 326 may be positioned in thecenter of central portion 302 extending in a longitudinal direction anda lateral end locating pin 329, best seen in FIGS. 29 and 31, may extendperpendicular to axis 303 in an anterior-posterior direction tofacilitate the location of implant 300 using fluoroscopic devices knownto those skilled in the art. Locating pins 326, 329 may be made from anyknown radio-opaque material known to those skilled in the art,including, but not limited to, tantalum.

As best seen in FIGS. 29 and 32, lateral end portion 306 generallycomprises a thin wall or plate having a uniform thickness 328. As shownin FIG. 32, when viewed from the end, end portion 306 has a generallyarcuate, bent, or teardrop shaped top or proximal end 330 and a roundedbottom or distal end 332 and a hexagonal opening 333 to accommodate orengage an insertion tool 424 (shown in FIGS. 39-41 and 50-52). Inalternate embodiments, any suitable attachment means known to thoseskilled in the art may be utilized to engage insertion tool 424 withimplant 300, including, but not limited to, a threaded engagement. Inone embodiment, opening 333 may extend through the entire body of theimplant, creating a cannulated body. The arcuate proximal end 330 isconfigured and dimensioned to accommodate positioning between spinousprocesses such that the anterior cutout or inner curve 334 of end 330 isshaped and sized to contact the lamina upon installation. Anterior curve334 in end portion 306 facilitates anterior positioning as it allowsimplant 300 to wrap around, accommodate or engage the lamina uponinstallation in an anterior position with respect to the spinousprocesses. In another embodiment, a similar sized and shaped anatomicalanterior cutout may be provided on first end portion 304. According toone embodiment, implant 300 is configured to be positioned in a finalinstallation location anterior the spinous processes. In this regard, inone embodiment implant 300 may be maintained or held in the installedposition without additional fixation devices. As best seen in FIG. 29,distal end 332 protrudes longitudinally beyond distal support surface310 in the distal direction. In one variation, the protruding distal end332 of second end portion 306 is configured to prevent over-insertion orover rotation of implant 300 when the implant is positioned into thefirst installation position. In one embodiment, a transition, ramp, orchamfer 336 is provided between end portion 306 and support portion 302.In another variation chamfer 336 comprises a generally linear transitionor pyramid-like step or increase from support portion 302 to end portion306. In general, chamfer 336 functions as a ramp or transition tofacilitate positioning or centering of the spinous process adjacentsupport surfaces 308, 310.

In certain variations of the aforementioned embodiment, implant 300 maybe attached to one or both of the adjacent spinous processes to securethe implant. By way of non-limiting example, the implant may have one ormore openings 335 which permit the attachment of the implant to one orboth spinous processes by one or more fastening devices, such as, forexample, a suture or screw. In another embodiment, one or moreadditional openings may be provided on the opposite end portion toaccommodate a fixation or fastening device.

In one embodiment, at least a portion of the front and back surfacescomprise textured, striated, or grooved portion(s) 337. In thisembodiment, portions 337 comprise multiple lateral grooves 339 extendinglaterally along a portion of the front and back surfaces of end portions304, 306. In operation, grooved portions 337 may prevent movement ofimplant 300 in any non-parallel direction with respect to any portion ofthe spinous processes that it may contact upon implantation. In thisregard, groove portions 337 facilitate mechanical fixation with respectto the spinous processes.

FIGS. 34-36 depict alternate implants 400, 405, 410 according to thepresent invention adapted to be placed between adjacent spinousprocesses. Implants 400, 405, 410 are similar to implant 300 of FIGS.28-33, except that the amount of lateral grooves may be more or lessthan lateral grooves 339 of implant 300. Referring to FIG. 34, in oneembodiment, implant 400 may comprise more grooves and as shown in FIG.36, in another embodiment, implant 410 may be free from groovesaltogether. Referring to FIG. 35, according to one embodiment, implant405 may comprise grooves along a majority of the front and back surfacesand may be positioned at an angle. According to another aspect of theinvention, implant 405 may comprise indented regions 407, 409 along thecentral support portion to accommodate or center a portion of thespinous processes therein. In one variation, proximal indented region407 may have a different width than distal indented region 409. In thisregard, the differing widths may accommodate differing contact widths ofadjacent processes on the posterior and distal sides upon implantation.According to one aspect of the present invention, multiple implants ofvarying groove arrangements may be provided in a kit for appropriateselection and installation by a surgeon.

Referring to FIGS. 37-38, another implant 420 according to the presentinvention is shown. Implant 420 is similar to implant 300 describedabove, except that central portion 422 has a circular cross-section witha generally constant diameter 423 along its lateral axis. In operation,diameter 423 provides a constant distraction distance and once theimplant is implanted and after the spinous processes are positionedadjacent central portion 422 of the implant 420, the implant maymaintain the spinous processes in a distracted or spaced condition, forexample where the distraction distance or diameter 423 of implant 420 isgreater than a pre-implantation distance between the spinous processes.According to one aspect of the present invention, multiple implantshaving varying cross-sectional shapes and sizes may be provided in a kitfor appropriate selection and installation by a surgeon. For example, incertain kits according to the invention, implants may be provided withheights ranging from about 8 mm to about 16 mm in 1 mm increments, andwidths ranging from about 12 mm to about 20 mm in 1 mm increments. Insome kits according to the invention, implants may be provided having adepth from about 6 mm to about 14 mm.

Referring to FIGS. 39-42 and 50-52, according to methods of the presentinvention, implants 300, 400, 410, 420 may be inserted between twoadjacent spinous processes 5 using an insertion tool 424. In oneembodiment, as best seen in FIG. 51, insertion tool 424 comprises ashaft 426 with a tip 428 extending generally at an angle 427 withrespect to shaft 426. In one variation, angle 427 may be between about100 and 135 degrees. As explained above, in one variation, tip 428comprises a hexagonal perimeter sized and shaped to engage a similarlyshaped opening on the implant, such as opening 333 shown in FIG. 32. Inalternate embodiments, any suitable attachment means known to thoseskilled in the art may be utilized to engage insertion tool 424 withimplant 300, including, but not limited to, a threaded engagement. Inone embodiment of a method according to the invention, as shown forexample in FIG. 39 for implant 300, a portion of end portion 304 maycontact at least one of the adjacent spinous processes. In onevariation, the implant may be inserted laterally such that the bull nosetip or distal end 318 of end portion 304 is inserted between adjacentspinous process and the implant may be laterally advanced and pivoted todilate or distract the processes until the implant is positioned into oradjacent the saddle or support portion 302 of the implant, as shown inFIG. 40. As shown in FIG. 40, the adjacent spinous processes may contactor engage front and back surfaces 309, 311 of support portion 302.Subsequently, in another embodiment, implant 300 may be rotated 90degrees to further distract the spinous process until the two adjacentspinous processes engage or contact the top and bottom support surfaces308, 310, as shown in FIG. 41. After insertion tool 424 is removed,implant 300 is positioned in a final implantation position as shown inFIG. 42.

As explained above with respect to other embodiments, in this embodimentthe implant itself may serve to dilate or distract the spinous processesas it is being inserted and/or after insertion. For example, the implantmay be initially inserted laterally and pivotally between the compressedadjacent spinous processes as shown in FIG. 39. In one embodiment, thesupraspinous ligament need not be removed. In operation, lateral endportion 304 of implant 300, engages the adjacent spinous processes asthe implant is inserted laterally and pivoted to act or perform in acam-like manner to translate the lateral/pivotal force to separate thespinous processes in the longitudinal or cranial-caudal direction as theimplant is inserted. For example, in an initial pre-implantationcondition, the adjacent spinous processes may be in an initialcompressed state such that the initial space or longitudinal distancebetween the processes may be equal to or smaller than distance 312 ofimplant 300. During lateral and pivotal insertion of implant 300, asshown in FIG. 39, proximal tip 318 of lateral end portion 304 of theimplant may contact one or both of the spinous processes 5 and mayinitially distract the processes. As the implant is inserted furtherbetween the spinous processes and pivoted, as explained above, thetapered surface portions 323, 325 may distract the spinous processesfurther apart from one another, until the implant is positioned into afirst implantation position (FIG. 40) and the spinous processes arefitted adjacent the front and back surfaces 309, 311 of saddle orsupport portion 302 of the implant. In one embodiment, implant 300 maybe rotated about 90 degrees about the lateral axis 303 from thehorizontal or lateral position shown in FIG. 40 to the vertical orlongitudinal position shown in FIG. 41 and the spinous processes arefitted into the upper and lower surfaces of saddle or support portion302 of the implant separated by distraction distance 312. In thisregard, in one embodiment, shaft 426 of insertion tool 424 is generallymovable within the realm of the incision created between about 45degrees on both sides of a lateral plane 429. After insertion tool 424is removed, implant 300 is positioned in a final implantation positionas shown in FIG. 42. Once the implant is implanted and after the spinousprocesses 5 are fitted into the saddle or support portion 302 of implant300, the implant may maintain the spinous processes in a distracted orspaced condition, for example where the distance 312 of the implant isgreater than a pre-implantation distance between the spinous processes.

According to one embodiment of a method according to the invention forinserting implant 300, the adjacent first and second spinal processesmay be accessed by various methods known by practitioners skilled in theart, for example, by accessing the spinous processes from at least onelateral side/unilateral, bilateral, or midline posterior approach.Certain methods of the present invention include removing or dilatingany interspinous ligaments in a position in which the implant is to beplaced in the patient prior to inserting the implant. In one exemplaryembodiment, a dilation tool 430 as shown in FIGS. 43-44 may be utilizedto dilate interspinous ligaments. For example, when using a unilateralapproach, dilation tool 430 is particularly well suited to access and/ordilate ligaments on the side of the spinous processes opposite theincision. The bullet or horn shaped end portion 304 further facilitatesinsertion through the dilation. In this regard, according to certainmethods of the invention, a unilateral approach may be used to installimplant 300 without removal of the supraspinous ligament.

Other embodiments of methods of the present invention may includedilating or distracting the spinous processes apart from one anotherbefore sizing and/or before inserting the implant. In one exemplaryembodiment, a distraction tool 440 as shown in FIGS. 45-46 may beutilized to distract spinous processes. In operation, the distal tips442 of distraction tool 440 may be inserted between adjacent processesand the handles 444 on the proximal end of the tool may be compressed tocause distal tips 442 to spread apart. As is known in the art, acompression dial 446 and measuring bar 448 may be provided to facilitatemeasurable and/or precise distraction.

In certain methods of installation, it may be desired or necessary toreduce a portion of one or more facet joints adjacent the implantationlocale. For example, in some patients inflamed or enlarged facet jointsmay impede or hinder a surgeon's ability to install an implant betweenthe spinous processes. In one exemplary embodiment, a reamer tool 460 asshown in FIG. 47-48 may be utilized in combination with a guide sleeve480, shown in FIG. 49, to remove, ream, or otherwise reduce at least aportion of the enlarged facet. In one embodiment, reamer 460 comprises aplurality of fluted cutting surfaces 462 adjacent its distal tip 464. Inone variation, cutting surfaces 462 extend radially around distal tip464. In operation, guide sleeve 480 may be inserted into the patient andthe distal tip 482 of the guide sleeve 480 is configured and dimensionedto fit on or engage a bulbous facet to be treated. Reamer tool 460 maythen be inserted into sleeve 480 such that distal tip 482 contacts thefacet and rotation of reamer tool 460 grinds, cuts, reams or otherwiseremoves material from the facet joint.

In another embodiment of a method according to the invention, sizing ofthe space between adjacent spinous processes (for example using trials)may be performed. In one exemplary embodiment, a trial 490 and insertiontool 424, shown in FIGS. 50-52, may be utilized to size the spacebetween adjacent processes. In one variation, trial 490 comprisesmultiple longitudinal indentations or markings 492 on at least a portionof central portion 494. Markings 492 provide visual indication whenviewed under fluoroscopy of the width of the spinous processes andfacilitate the surgeon's selection of an appropriately sized implant.Similarly, the appropriate diameter of central portion 494 of trial 490may be selected to gauge the amount of distraction desired. In thisregard, the spacing of the spinous processes may be viewed underfluoroscopy to facilitate the surgeon's selection of an appropriatelysized implant. Finally, an implant of the appropriate size may beinserted between the adjacent spinous processes.

While the invention herein disclosed has been described by means ofspecific embodiments and applications thereof, numerous modificationsand variations can be made thereto by those skilled in the art withoutdeparting from the scope of the invention.

1. A prosthetic device for implantation between adjacent vertebralbodies in a vertebral column, the prosthetic device comprising: a bodycomprising a central support portion having top, bottom, front and backsurfaces, the central support portion extending laterally along alateral axis between first and second end portions, the first endportion extending longitudinally along a first longitudinal axis and thesecond end portion extending longitudinally along a second longitudinalaxis, and the first and second longitudinal axes are generallyperpendicular to the lateral axis, wherein at least a portion of firstand second end portions protrude beyond the top and bottom surfaces ofthe support portion in the cranial-caudal direction, protrude beyond thefront and the back surfaces of the support portion in theanterior-posterior direction to further distract at least a portion ofthe adjacent vertebral bodies of the vertebral column, and wherein thecentral support portion has first and second concave portions extendingfrom the first end portion to the second end portion on the upper andlower surfaces for supporting the adjacent vertebral bodies and thirdand fourth concave portions extending from the first end portion to thesecond end portion on the front and back surfaces for supporting andcentering the adjacent vertebral bodies on the central support portion,wherein the second end portion comprises a plate having a uniformthickness and an opening to engage an insertion tool, the openingextending from the second end portion through the central supportportion and the first end portion.
 2. The device of claim 1, wherein thebody is made from a polyetheretherketone (PEEK) material.
 3. The deviceof claim 1, wherein the body includes a locating pin, the locating pinmade from a radio-opaque material.
 4. The device of claim 1, wherein thefirst end portion is curved adjacent a distal end.
 5. The device ofclaim 1, wherein the support portion is configured and dimensioned tofit between adjacent spinous processes and further comprises: a proximalsupport surface spaced longitudinally from a distal support surface by afirst distance, the support surfaces configured to contact adjacentspinous processes of the vertebral column, wherein the first distance ispredetermined for spacing of two adjacent spinous processes when thedevice is implanted in the vertebral column.
 6. The device of claim 1,wherein the support portion has a generally circular cross-section. 7.The device of claim 1, wherein the support portion has a generallyrectangular cross-section.
 8. The device of claim 1, wherein at least aportion of the end portions extend longitudinally beyond first andsecond support surfaces in the longitudinal direction.
 9. The device ofclaim 1, wherein the first and second longitudinal axes are coplanar tothe lateral axis.
 10. The device of claim 1, wherein the end portionsare laterally spaced by a second distance, the second distance generallycorresponding to a predetermined distance for accommodating the width ofthe spinous processes.
 11. The device of claim 1, wherein the endportions are configured and dimensioned to contact the lateral sides ofthe spinous process when the device is implanted in the vertebralcolumn.
 12. The device of claim 1, wherein at least one of the endportions define at least one opening for accommodating a fasteningdevice to fasten the device to the spinous process when the device isimplanted.
 13. The device of claim 1, wherein the body is configured anddimensioned to be rotated in-situ to distract adjacent spinousprocesses.
 14. The device of claim 1, wherein at least one of the firstand second end portions comprise an anterior cutout to accommodate thelamina in an implanted position.
 15. The device of claim 1, wherein thesupport portion further comprises a ramp portion adjacent at least oneend portion to center the adjacent spinous processes along the centralportion.
 16. A prosthetic device for implantation in a treated area ofan intervertebral space between vertebral bodies of a spine, comprising:a spacer body comprising a central support portion extending along alateral axis between first and second end portions, the central supportportion comprising an anterior surface and a posterior surface, whereinthe anterior and posterior surfaces each have a contact area capable ofengaging with anatomy in the treated area and the anterior and posteriorsurfaces are spaced apart a first distraction distance in a firstdirection, the central support portion comprising an inferior surfaceand a superior surface, wherein the inferior and superior surfaces eachhave a contact area capable of engaging with anatomy in the treated areaand the inferior and superior surfaces are spaced apart a seconddistraction distance in a second direction, wherein the firstdistraction distance is less than the second distraction distance,wherein the central support portion is configured and dimensioned to bepositioned between adjacent vertebral bodies, wherein when the device isin a first implantation position the adjacent vertebral bodies aremaintained substantially separated by at least the first distractiondistance and when the device is in a second implantation position theadjacent vertebral bodies are maintained substantially separated by atleast the second distraction distance, wherein the central supportportion is rotatable from the first implantation position to the secondimplantation position, wherein in the first implantation position thefirst and second end portions are located between the adjacent vertebralbodies, extending in an anterior-posterior direction, wherein in thesecond implantation position the first and second end portions arelocated laterally adjacent opposite lateral sides of a portion of thevertebral bodies, extending in a cranial-caudal direction, wherein atleast a portion of the contact areas of the anterior and posteriorsurfaces are concave for engaging the adjacent vertebral bodies and atleast a portion of the contact areas of the inferior and superiorsurfaces are concave for engaging the adjacent vertebral bodies, andwherein at least a portion of first and second end portions protrudebeyond the superior and inferior surfaces of the central support portionin a cranial-caudal direction and protrude beyond the anterior and theposterior surfaces of the support portion in an anterior-posteriordirection to further distract at least a portion of the adjacentvertebral bodies of the vertebral column, wherein the first and secondend portions further comprise multiple grooves extending laterally alonga portion of the front and back surface of the first and second endportions for preventing movement in any non-parallel direction withrespect to the spinous processes.
 17. The device of claim 16, whereinthe first end portion extends longitudinally along a first longitudinalaxis and the second end portion extends longitudinally along a secondlongitudinal axis, and the first and second longitudinal axes aregenerally perpendicular to the lateral axis.
 18. The device of claim 17,wherein the first end portion is tapered along its longitudinal length.19. The device of claim 16, wherein at least one of the first and secondend portions comprise an anterior cutout to accommodate a portion of thelamina in the second implantation position.
 20. The device of claim 16,wherein the support portion further comprises a ramp portion adjacent atleast one end portion to center a portion of the adjacent vertebralbodies along the central portion.
 21. A prosthetic device forimplantation between adjacent spinous processes in a vertebral column,the prosthetic device comprising: a body comprising a central supportportion extending laterally along a lateral axis between first andsecond end portions, the first end portion extending longitudinallyalong a first longitudinal axis and the second end portion extendinglongitudinally along a second longitudinal axis, and the first andsecond longitudinal axes are substantially perpendicular to the lateralaxis, wherein at least a portion of first and second end portionsprotrude beyond a top surface and a bottom surface of the supportportion in the cranial-caudal direction and protrude beyond a frontsurface and a back surface of the support portion in theanterior-posterior direction to further distract at least a portion ofthe adjacent spinous processes of the vertebral column, wherein thesupport portion is configured and dimensioned to fit between adjacentspinous processes and further comprises a concave proximal supportsurface spaced longitudinally from a distal concave support surface by afirst distance, the support surfaces configured to contact and supportadjacent spinous processes of the vertebral column, wherein the firstdistance is predetermined for spacing of two adjacent spinous processeswhen the device is implanted in the vertebral column, wherein the secondend portion comprises an anterior cutout to accommodate a portion of thelamina when the device is implanted in the vertebral column and includesat least one opening to accommodate a fastening device to fasten thedevice to the spinous process when the device is implanted in thevertebral column, and wherein the first and second end portions furthercomprise multiple grooves extending laterally along a portion of thefront and back surface of the first and second end portions forpreventing movement in any non-parallel direction with respect to thespinous processes wherein the central support portion comprises proximalindented regions and distal indented regions, the width of the proximalindented regions being different than the width of the distal indentedregions.